ClinVar Miner

Submissions for variant NM_006186.4(NR4A2):c.854G>A (p.Gly285Asp)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues RCV002795916 SCV003035415 likely pathogenic Complex neurodevelopmental disorder 2022-06-10 criteria provided, single submitter clinical testing

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